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Variant : CV161039 (GRCh37/hg19 12p13.33(chr12:70794-230421)x3) Homo sapiens

Symbol: CV161039
Name: GRCh37/hg19 12p13.33(chr12:70794-230421)x3
Condition: See cases [RCV000140010]
Clinical Significance: benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: IQSEC3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000012.11:g.(?_70794)_(230421_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh371270,794 - 230,421CLINVAR
Build 361216,001 - 100,682CLINVAR
Cytogenetic Map1212p13.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487540
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-14
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.